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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 20, 2001
Frequent inactivation of the TP53 gene in esophageal squamous cell carcinoma from a high-risk population in ChinaN Hu, J Huang, M R Emmert-Buck, et al.Cancer Detection and Prevention|April 3, 2003
Common genetic variants of TP53 and BRCA2 in esophageal cancer patients and healthy individuals from low and high risk areas of northern ChinaNan Hu, Wen-Jun Li, Hua Su, et al.Genes, Chromosomes & Cancer|January 27, 1998
Allelic imbalance, including deletion of PTEN/MMACI, at the Cowden disease locus on 10q22-23, in hamartomas from patients with Cowden syndrome and germline PTEN mutationD J Marsh, P L Dahia, V Coulon, et al.British Journal of Cancer|June 10, 2011
Epstein-Barr virus microRNAs and lung cancerJ Koshiol, M L Gulley, Y Zhao, et al.Diabetes, Obesity & Metabolism|February 16, 2016
Prevention of antibiotic-associated metabolic syndrome in mice by intestinal alkaline phosphataseK P Economopoulos, N L Ward, C D Phillips, et al.Journal of Medical Genetics|January 8, 2008
CDKN2A mutations and melanoma risk in the Icelandic populationA M Goldstein, S N Stacey, J H Olafsson, et al.Cell|June 14, 1996
Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndromeH Hahn, C Wicking, P G Zaphiropoulous, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|May 16, 2019
Associations of pigmentary and naevus phenotype with melanoma risk in two populations with comparable ancestry but contrasting levels of ambient sun exposureA E Cust, M Drummond, D T Bishop, et al.Nature Genetics|May 1, 1996
Localization of the gene for Cowden disease to chromosome 10q22-23M R Nelen, G W Padberg, E A Peeters, et al.British Journal of Cancer|January 31, 2013
Common genetic variants in the 9p21 region and their associations with multiple tumoursF Gu, R M Pfeiffer, S Bhattacharjee, et al.Pageof 15